Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: Magea9 ENSRNOG00000023016

.

Description

MAGE family member A9 [Source:RGD Symbol;Acc:1565494]

Gene Synonyms

MGC114427

Location

Primary_assembly X: 147,655,721-147,661,093 forward strand.

GRCr8:CM070411.1

About this gene

This gene has 2 transcripts (splice variants), 173 orthologues, 34 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000102737.2	Magea9-202	1865	300aa	ENSRNOP00000082572.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZXB3 Q4V8H6	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSRNOT00000037881.6	Magea9-201	1676	300aa	ENSRNOP00000053408.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZXB3 Q4V8H6	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

.

Summary

.

.